Related Experiment Video
Updated: Jun 13, 2026

Preparation and Characterization of C60/Graphene Hybrid Nanostructures
Published on: May 15, 2018
Soluble chlorofullerenes C(60)Cl(2,4,6,8,10). Synthesis, purification, compositional analysis, stability, and
Igor V Kuvychko1, Alexey V Streletskii, Natalia B Shustova
1Department of Chemistry, Colorado State University, Fort Collins, Colorado 80523, USA.
Abstract:
The efficacy of various analytical techniques for the characterization of products of C(60) chlorination reactions were evaluated by (i) using samples of C(60)Cl(6) of known purity and (ii) repeating a number of literature syntheses reported to yield pure C(60)Cl(n) compounds. The techniques were NMR, UV-vis, IR, and Raman spectroscopy, FAB, MALDI, LDI, ESI, and APCI mass spectrometry, HPLC, TGA, elemental analysis, and single-crystal X-ray diffraction. Most of these techniques are shown to give ambiguous or erroneous results, calling into question the composition and/or purity of nearly all C(60)Cl(n) compounds reported to date. The optimum analytical method for chlorofullerenes was found to be a combination of HPLC and either MALDI or APCI mass spectrometry. For the first time, the chlorination of C(60) by ICl, ICl(3), and Cl(2) was studied in detail using dynamic HPLC analysis and APCI mass spectrometry. Suitable conditions were found for the preparation of the new chlorofullerenes 1,7-C(60)Cl(2), 1,9-C(60)Cl(2), 1,6,9,18-C(60)Cl(4), and 1,2,7,10,14,24,25,28,29,31-C(60)Cl(10). The latter compound was also studied by (13)C NMR spectroscopy and X-ray diffraction, which led to the unambiguous determination of its asymmetric addition pattern. The unusual structure of C(60)Cl(10) was compared with other possible isomers using DFT-predicted relative energies. These results, along with additional experimental data and an analysis of the DFT-predicted frontier orbitals of likely intermediates, were used to rationalize the formation of the new compound C(60)Cl(10) from C(60)Cl(6) and excess ICl without the rearrangement of any C-Cl bonds. For the first time, the stability of C(60)Cl(n) compounds under a variety of conditions was studied in detail, leading to the discovery that they are, in general, very light-sensitive in solution. The X-ray structure of C(60)Cl(6) was also redetermined with higher precision.
More Related Videos
09:35Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
Published on: September 18, 2016
06:55Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
Published on: September 26, 2016
Related Concept Videos
Stability of Substituted Cyclohexanes
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
Halogenation of Alkenes
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
Chair Conformation of Cyclohexane
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this staggered...
Conformations of Cyclohexane
The chair form is the most stable and derives its name from its resemblance to the “easy chair.” In the chair conformation, two carbon atoms are arranged out-of-plane — one above and one below, minimizing the torsional strain. In the chair form, the bond angle is very close to the ideal tetrahedral value,...
Structure of Conjugated Dienes
Conjugated dienes are compounds characterized by the presence of alternating double and single bonds. In a conjugated system like 1,3-butadiene, the unhybridized 2p orbital on each carbon overlaps continuously, allowing the π electrons to be delocalized across the entire molecule. In contrast, this type of overlap does not occur in cumulated and isolated dienes, such as 2,3-pentadiene and 1,4-pentadiene, respectively. Instead, the π electrons remain localized between the double...
Predicting Molecular Geometry